<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Medical Laboratory Journal</title>
<title_fa>Medical Laboratory Journal</title_fa>
<short_title>mljgoums</short_title>
<subject>Medical Sciences</subject>
<web_url>http://mlj.goums.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2538-4449</journal_id_issn>
<journal_id_issn_online>2538-4449</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.61186/mlj</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1405</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2026</year>
	<month>6</month>
	<day>1</day>
</pubdate>
<volume>20</volume>
<number>2</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Optimum cultural conditions to achieve the best biofilm formation and high level icaA transcription by Staphylococcus aureus</title>
	<subject_fa>ميکروب شناسي</subject_fa>
	<subject>Microbiology</subject>
	<content_type_fa>Research Article</content_type_fa>
	<content_type>Research Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;span style=&quot;line-height:200%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;color:black&quot;&gt;&lt;b&gt;Abstract &lt;/b&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;span style=&quot;line-height:200%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;color:black&quot;&gt;&lt;b&gt;Background:&lt;/b&gt; Biofilm formation in&amp;nbsp;&lt;i&gt;Staphylococcus aureus &lt;/i&gt;(&lt;i&gt;S. aureus&lt;/i&gt;), mediated by the&amp;nbsp;&lt;i&gt;ica&lt;/i&gt;&amp;nbsp;operon, is a key virulence factor. This study examined how different glucose-supplemented broth culture media influence biofilm production and&amp;nbsp;&lt;i&gt;ica&lt;/i&gt;&amp;nbsp;gene expression in&amp;nbsp;&lt;i&gt;S. aureus&lt;/i&gt;.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;span style=&quot;line-height:200%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;color:black&quot;&gt;&lt;b&gt;Methods:&lt;/b&gt; The phenotypic ability to adhere to a polystyrene surface and to produce slime layer were evaluated using &lt;span style=&quot;line-height:200%&quot;&gt;microtiter plate test (&lt;/span&gt;MtP) and Congo red tube test, respectively. Using PCR, the presence of intercellular adhesion (&lt;i&gt;ica&lt;/i&gt;) locus&lt;i&gt; &lt;/i&gt;in &lt;i&gt;S. aureus&lt;/i&gt; strains was confirmed and subsequently, quantitative real-time RT-PCR was performed to investigate transcription of &lt;i&gt;icaA&lt;/i&gt; in various media including Tryptic soy broth (TSB), Brain-heart infusion broth (BHIB), (Nutrient broth) NB and (Muller-Hinton broth) MHB contained 0, 0.25, 0.5, 1 and 2% glucose.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;span style=&quot;line-height:200%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;color:black&quot;&gt;&lt;b&gt;Results:&lt;/b&gt; Our results showed that although all of the studied strains adhered to the wells of polystyrene microtiter plates, the optimum rate of biofilm formation was observed for TSB medium contained 1% glucose, but biofilm formation was not significantly different in NB, MHB and BHIB media. Supplementation of all media with 1% glucose led to the highest production of biofilm formation and in all media transcription of &lt;i&gt;icaA&lt;/i&gt; was increased with glucose addition to one present.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;b&gt;&lt;span lang=&quot;EN-GB&quot; style=&quot;font-size:11.0pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span calibri=&quot;&quot; style=&quot;font-family:&quot;&gt;Conclusions:&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/b&gt; &lt;span lang=&quot;TR&quot; style=&quot;font-size:11.0pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span calibri=&quot;&quot; style=&quot;font-family:&quot;&gt;The results of the present study indicated that TSB medium supplemented with 1% glucose was the most appropriate medium for evaluation of biofilm formation by &lt;i&gt;S. aureus&lt;/i&gt; isolates.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Biofilm formation, Staphylococcus aureus, Culture media, glucose, quantitative real-time RT-PCR</keyword>
	<start_page>0</start_page>
	<end_page>0</end_page>
	<web_url>http://mlj.goums.ac.ir/browse.php?a_code=A-10-1738-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Aram</first_name>
	<middle_name></middle_name>
	<last_name>Sharifi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>a.sharifi@uok.ac.ir</email>
	<code>100319475328460032405</code>
	<orcid>100319475328460032405</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Animal Science, Faculty of Agriculture, University of Kurdistan, Sanandaj, Kurdistan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Abdolmajid</first_name>
	<middle_name></middle_name>
	<last_name>Mohammadzadeh</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>Mohammadzadeh@basu.ac.ir</email>
	<code>100319475328460032406</code>
	<orcid>100319475328460032406</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Pathobiology, Faculty of Veterinary Science, Bu-Ali Sina University, Hamedan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Pezhman</first_name>
	<middle_name></middle_name>
	<last_name>Mahmoodi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>mahmoodi_pezhman@yahoo.com</email>
	<code>100319475328460032407</code>
	<orcid>100319475328460032407</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Pathobiology, Faculty of Veterinary Science, Bu-Ali Sina University, Hamedan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Taghi</first_name>
	<middle_name></middle_name>
	<last_name>Zahraei Salehi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>tsalehi@ut.ac.ir</email>
	<code>100319475328460032408</code>
	<orcid>100319475328460032408</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Microbiology and Immunology, Faculty of Veterinary Science, Tehran University, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
